JP2004527560A5 - - Google Patents
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- Publication number
- JP2004527560A5 JP2004527560A5 JP2002585423A JP2002585423A JP2004527560A5 JP 2004527560 A5 JP2004527560 A5 JP 2004527560A5 JP 2002585423 A JP2002585423 A JP 2002585423A JP 2002585423 A JP2002585423 A JP 2002585423A JP 2004527560 A5 JP2004527560 A5 JP 2004527560A5
- Authority
- JP
- Japan
- Prior art keywords
- cyclopentylamino
- pyrazolo
- pyridin
- pyrimidinyl
- fluorophenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 125000006312 cyclopentyl amino group Chemical group [H]N(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 30
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims 23
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 21
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 6
- 125000003342 alkenyl group Chemical group 0.000 claims 6
- -1 1-pyrrolidinylcarbonyl Chemical group 0.000 claims 5
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 5
- 125000005843 halogen group Chemical group 0.000 claims 5
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims 4
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 3
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 125000006317 cyclopropyl amino group Chemical group 0.000 claims 3
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims 3
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 claims 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000012453 solvate Substances 0.000 claims 2
- RJAIATRJLAYBKS-UHFFFAOYSA-N 4-[5-chloro-3-[2-(cyclopentylamino)pyrimidin-4-yl]-7-(cyclopropylamino)pyrazolo[1,5-a]pyridin-2-yl]phenol Chemical compound C1=CC(O)=CC=C1C1=NN(C(NC2CC2)=CC(Cl)=C2)C2=C1C1=CC=NC(NC2CCCC2)=N1 RJAIATRJLAYBKS-UHFFFAOYSA-N 0.000 claims 1
- WNWVKZTYMQWFHE-UHFFFAOYSA-N 4-ethylmorpholine Chemical group [CH2]CN1CCOCC1 WNWVKZTYMQWFHE-UHFFFAOYSA-N 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- CNMBLWDXHYWTLA-UHFFFAOYSA-N 5-chloro-3-[2-(cyclopentylamino)pyrimidin-4-yl]-n-cyclopropyl-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-7-amine Chemical compound C1=CC(OC)=CC=C1C1=NN(C(NC2CC2)=CC(Cl)=C2)C2=C1C1=CC=NC(NC2CCCC2)=N1 CNMBLWDXHYWTLA-UHFFFAOYSA-N 0.000 claims 1
- WCKXXYWOSVAGLZ-UHFFFAOYSA-N 5-chloro-3-[2-(cyclopentylamino)pyrimidin-4-yl]-n-cyclopropyl-2-[4-(cyclopropylmethoxy)phenyl]pyrazolo[1,5-a]pyridin-7-amine Chemical compound N12N=C(C=3C=CC(OCC4CC4)=CC=3)C(C=3N=C(NC4CCCC4)N=CC=3)=C2C=C(Cl)C=C1NC1CC1 WCKXXYWOSVAGLZ-UHFFFAOYSA-N 0.000 claims 1
- GLKWTXUVFUJIGX-UHFFFAOYSA-N 5-chloro-n-cyclopentyl-2-(4-methoxyphenyl)-3-(2-methylsulfanylpyrimidin-4-yl)pyrazolo[1,5-a]pyridin-7-amine Chemical compound C1=CC(OC)=CC=C1C1=NN(C(NC2CCCC2)=CC(Cl)=C2)C2=C1C1=CC=NC(SC)=N1 GLKWTXUVFUJIGX-UHFFFAOYSA-N 0.000 claims 1
- KMUNEVPPFFIIAM-UHFFFAOYSA-N 5-chloro-n-cyclopentyl-2-(4-methoxyphenyl)-3-(2-methylsulfinylpyrimidin-4-yl)pyrazolo[1,5-a]pyridin-7-amine Chemical compound C1=CC(OC)=CC=C1C1=NN(C(NC2CCCC2)=CC(Cl)=C2)C2=C1C1=CC=NC(S(C)=O)=N1 KMUNEVPPFFIIAM-UHFFFAOYSA-N 0.000 claims 1
- FVDIJBUKMLLPCL-UHFFFAOYSA-N 5-chloro-n-cyclopentyl-3-[2-(cyclopentylamino)pyrimidin-4-yl]-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-7-amine Chemical compound C1=CC(F)=CC=C1C1=NN(C(NC2CCCC2)=CC(Cl)=C2)C2=C1C1=CC=NC(NC2CCCC2)=N1 FVDIJBUKMLLPCL-UHFFFAOYSA-N 0.000 claims 1
- ARFXCYCTFNKRNL-UHFFFAOYSA-N 5-chloro-n-cyclopentyl-3-[2-(cyclopentylamino)pyrimidin-4-yl]-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-7-amine Chemical compound C1=CC(OC)=CC=C1C1=NN(C(NC2CCCC2)=CC(Cl)=C2)C2=C1C1=CC=NC(NC2CCCC2)=N1 ARFXCYCTFNKRNL-UHFFFAOYSA-N 0.000 claims 1
- KVWGXHFUCADPDK-UHFFFAOYSA-N 5-chloro-n-cyclopentyl-3-[2-(cyclopropylamino)pyrimidin-4-yl]-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-7-amine Chemical compound C1=CC(OC)=CC=C1C1=NN(C(NC2CCCC2)=CC(Cl)=C2)C2=C1C1=CC=NC(NC2CC2)=N1 KVWGXHFUCADPDK-UHFFFAOYSA-N 0.000 claims 1
- ZIDVGKZMRABSOF-UHFFFAOYSA-N 7-(cyclopentylamino)-3-[2-(cyclopentylamino)pyrimidin-4-yl]-2-(4-fluorophenyl)-n-hydroxypyrazolo[1,5-a]pyridine-6-carboxamide Chemical compound ONC(=O)C=1C=CC2=C(C=3N=C(NC4CCCC4)N=CC=3)C(C=3C=CC(F)=CC=3)=NN2C=1NC1CCCC1 ZIDVGKZMRABSOF-UHFFFAOYSA-N 0.000 claims 1
- RWOYMYIYXMICCH-UHFFFAOYSA-N 7-chloro-n-cyclopentyl-3-[2-(cyclopentylamino)pyrimidin-4-yl]-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-5-amine Chemical compound C1=CC(F)=CC=C1C1=NN(C(Cl)=CC(NC2CCCC2)=C2)C2=C1C1=CC=NC(NC2CCCC2)=N1 RWOYMYIYXMICCH-UHFFFAOYSA-N 0.000 claims 1
- 101100240516 Caenorhabditis elegans nhr-10 gene Proteins 0.000 claims 1
- 101100079984 Caenorhabditis elegans nhr-9 gene Proteins 0.000 claims 1
- 208000029433 Herpesviridae infectious disease Diseases 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- FQNJTEQMAQMIMU-UHFFFAOYSA-N [7-(cyclopentylamino)-3-[2-(cyclopentylamino)pyrimidin-4-yl]-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-6-yl]methanol Chemical compound OCC=1C=CC2=C(C=3N=C(NC4CCCC4)N=CC=3)C(C=3C=CC(F)=CC=3)=NN2C=1NC1CCCC1 FQNJTEQMAQMIMU-UHFFFAOYSA-N 0.000 claims 1
- 150000001540 azides Chemical class 0.000 claims 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- JQTSLEMPHVXCDY-UHFFFAOYSA-N ethyl 7-(cyclopentylamino)-3-[2-(cyclopentylamino)pyrimidin-4-yl]-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine-6-carboxylate Chemical compound CCOC(=O)C=1C=CC2=C(C=3N=C(NC4CCCC4)N=CC=3)C(C=3C=CC(F)=CC=3)=NN2C=1NC1CCCC1 JQTSLEMPHVXCDY-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- OJDKXSZDDHEORF-UHFFFAOYSA-N n-cyclopentyl-2-(4-fluorophenyl)-3-(2-pyrrolidin-1-ylpyrimidin-4-yl)-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-7-amine Chemical compound C1=CC(F)=CC=C1C1=NN(C(NC2CCCC2)=C(C=C2)C(F)(F)F)C2=C1C1=CC=NC(N2CCCC2)=N1 OJDKXSZDDHEORF-UHFFFAOYSA-N 0.000 claims 1
- ZKYXVDDZBFULBP-UHFFFAOYSA-N n-cyclopentyl-4-[5,7-dichloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]pyrimidin-2-amine Chemical compound C1=CC(F)=CC=C1C1=NN(C(Cl)=CC(Cl)=C2)C2=C1C1=CC=NC(NC2CCCC2)=N1 ZKYXVDDZBFULBP-UHFFFAOYSA-N 0.000 claims 1
- UPURSWNGJDCEHG-UHFFFAOYSA-N n-cyclopentyl-4-[5,7-dichloro-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-3-yl]pyrimidin-2-amine Chemical compound C1=CC(OC)=CC=C1C1=NN(C(Cl)=CC(Cl)=C2)C2=C1C1=CC=NC(NC2CCCC2)=N1 UPURSWNGJDCEHG-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28694801P | 2001-04-27 | 2001-04-27 | |
| PCT/US2002/010687 WO2002088124A2 (en) | 2001-04-27 | 2002-04-05 | Pyrazolo'1,5-a!pyridine derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004527560A JP2004527560A (ja) | 2004-09-09 |
| JP2004527560A5 true JP2004527560A5 (https=) | 2005-08-18 |
Family
ID=23100830
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002585423A Pending JP2004527560A (ja) | 2001-04-27 | 2002-04-05 | ピラゾロ［１，５−α］ピリジン誘導体 |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US6962914B2 (https=) |
| EP (1) | EP1385847B1 (https=) |
| JP (1) | JP2004527560A (https=) |
| AT (1) | ATE296826T1 (https=) |
| AU (1) | AU2002305143A1 (https=) |
| DE (1) | DE60204452T2 (https=) |
| ES (1) | ES2242028T3 (https=) |
| WO (1) | WO2002088124A2 (https=) |
Families Citing this family (53)
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|---|---|---|---|---|
| PE20020506A1 (es) * | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | Derivados de pirazol fusionados como inhibidores de la proteina cinasa |
| DE60112330T2 (de) * | 2000-12-15 | 2006-04-13 | Glaxo Group Ltd., Greenford | Pyrazolopyridinderivate |
| EP1366048B1 (en) * | 2001-03-08 | 2004-08-25 | SmithKline Beecham Corporation | Pyrazolopyridine derivatives |
| JP4219171B2 (ja) * | 2001-04-10 | 2009-02-04 | スミスクライン ビーチャム コーポレーション | 抗ウイルス性ピラゾロピリジン化合物 |
| DE60220525T2 (de) * | 2001-09-07 | 2008-02-07 | Smithkline Beecham Corp. | Pyrazolo-pyridine für die behandlung von herpes-ansteckungen |
| JP2005516916A (ja) * | 2001-12-11 | 2005-06-09 | スミスクライン ビーチャム コーポレーション | 抗ヘルペス薬としてのピラゾロ−ピリジン誘導体 |
| AU2003217712A1 (en) | 2002-03-07 | 2003-09-22 | Smithkline Beecham Corporation | Pyrazolopyrimidine and pyrazolotriazine derivatives and pharmaceutical compositions containing them |
| WO2006055245A2 (en) * | 2004-11-17 | 2006-05-26 | Smithkline Beecham Corporation | Process for preparing pyrazolopyridine compounds |
| US7812022B2 (en) * | 2004-12-21 | 2010-10-12 | Glaxosmithkline Llc | 2-pyrimidinyl pyrazolopyridine ErbB kinase inhibitors |
| CN101326182B (zh) * | 2005-12-05 | 2011-09-28 | 史密丝克莱恩比彻姆公司 | 2-嘧啶基吡唑并吡啶ErbB激酶抑制剂 |
| UA103319C2 (en) | 2008-05-06 | 2013-10-10 | Глаксосмитклайн Ллк | Thiazole- and oxazole-benzene sulfonamide compounds |
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| US8680108B2 (en) * | 2009-12-18 | 2014-03-25 | Incyte Corporation | Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors |
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| AR081810A1 (es) | 2010-04-07 | 2012-10-24 | Bayer Cropscience Ag | Piridinilpirazoles biciclicos |
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| EP2655374B1 (en) | 2010-12-20 | 2019-10-23 | Incyte Holdings Corporation | N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors |
| CA2825825A1 (en) * | 2011-01-27 | 2012-08-02 | The Trustees Of Princeton University | Inhibitors of mtor kinase as anti-viral agents |
| US9108984B2 (en) | 2011-03-14 | 2015-08-18 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors |
| WO2012135009A1 (en) | 2011-03-25 | 2012-10-04 | Incyte Corporation | Pyrimidine-4,6-diamine derivatives as pi3k inhibitors |
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-
2002
- 2002-04-05 AT AT02733945T patent/ATE296826T1/de not_active IP Right Cessation
- 2002-04-05 AU AU2002305143A patent/AU2002305143A1/en not_active Abandoned
- 2002-04-05 JP JP2002585423A patent/JP2004527560A/ja active Pending
- 2002-04-05 DE DE60204452T patent/DE60204452T2/de not_active Expired - Fee Related
- 2002-04-05 US US10/473,751 patent/US6962914B2/en not_active Expired - Fee Related
- 2002-04-05 EP EP02733945A patent/EP1385847B1/en not_active Expired - Lifetime
- 2002-04-05 WO PCT/US2002/010687 patent/WO2002088124A2/en not_active Ceased
- 2002-04-05 ES ES02733945T patent/ES2242028T3/es not_active Expired - Lifetime
-
2005
- 2005-03-31 US US11/095,212 patent/US7030134B2/en not_active Expired - Fee Related
- 2005-03-31 US US11/095,361 patent/US20050192295A1/en not_active Abandoned
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